Canonical Allele Identifier: CA366242364

Gene: ARID1B

Linked Data

• MyVariant Identifiers: chr6:g.157522400T>G (hg19) ; chr6:g.157201266T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.157201266T>G , CM000668.2:g.157201266T>G	GRCh38
NC_000006.11:g.157522400T>G , CM000668.1:g.157522400T>G	GRCh37
NC_000006.10:g.157564092T>G	NCBI36
NG_032093.1:g.428337T>G
NG_032093.2:g.428337T>G
NG_066624.1:g.430241T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000350026.11:c.4882T>G	ENSP00000055163.8:p.Ser1628Ala
ENST00000414678.8:c.4951T>G	ENSP00000412835.3:p.Ser1651Ala
ENST00000637015.2:c.5170T>G	ENSP00000489729.2:p.Ser1724Ala
ENST00000346085.10:c.4921T>G	ENSP00000344546.5:p.Ser1641Ala
ENST00000350026.10:c.4633T>G	ENSP00000055163.7:p.Ser1545Ala
ENST00000414678.7:c.3199T>G	ENSP00000412835.2:p.Ser1067Ala
ENST00000635849.1:c.2362T>G	ENSP00000490948.1:p.Ser788Ala
ENST00000635957.1:c.1993T>G	ENSP00000490385.1:p.Ser665Ala
ENST00000636227.1:n.3504T>G
ENST00000636254.1:n.961T>G
ENST00000636930.2:c.5041T>G MANE Select	ENSP00000490491.2:p.Ser1681Ala
ENST00000636940.1:n.3038T>G
ENST00000637015.1:c.2409T>G
ENST00000637568.1:c.2323T>G
ENST00000637741.1:n.1707T>G
ENST00000637810.1:c.2383T>G	ENSP00000489636.1:p.Ser795Ala
ENST00000637904.1:c.2542T>G	ENSP00000490550.1:p.Ser848Ala
ENST00000647938.1:c.4672T>G	ENSP00000498155.1:p.Ser1558Ala
ENST00000346085.9:c.4672T>G	ENSP00000344546.4:p.Ser1558Ala
ENST00000350026.9:c.4633T>G	ENSP00000055163.7:p.Ser1545Ala
ENST00000414678.6:c.3199T>G	ENSP00000412835.2:p.Ser1067Ala
NM_017519.2:c.4633T>G	NP_059989.2:p.Ser1545Ala
NM_020732.3:c.4672T>G	NP_065783.3:p.Ser1558Ala
XM_005267069.3:c.4792T>G	XP_005267126.2:p.Ser1598Ala
XM_011535984.1:c.3871T>G	XP_011534286.1:p.Ser1291Ala
XM_011535985.1:c.3691T>G	XP_011534287.1:p.Ser1231Ala
XM_011535986.1:c.3451T>G	XP_011534288.1:p.Ser1151Ala
XM_011535987.1:c.3070T>G	XP_011534289.1:p.Ser1024Ala
XM_011535988.1:c.1933T>G	XP_011534290.1:p.Ser645Ala
NM_001346813.1:c.4792T>G	NP_001333742.1:p.Ser1598Ala
NM_001363725.1:c.2542T>G	NP_001350654.1:p.Ser848Ala
XM_011535984.2:c.5002T>G	XP_011534286.2:p.Ser1668Ala
XM_011535988.3:c.1933T>G	XP_011534290.1:p.Ser645Ala
XM_017011103.2:c.4903T>G	XP_016866592.1:p.Ser1635Ala
XM_017011104.1:c.4873T>G	XP_016866593.1:p.Ser1625Ala
XM_017011105.2:c.4843T>G	XP_016866594.1:p.Ser1615Ala
XM_017011106.2:c.4714T>G	XP_016866595.1:p.Ser1572Ala
XM_017011107.2:c.4693T>G	XP_016866596.1:p.Ser1565Ala
XR_002956289.1:n.4988T>G
NM_001363725.2:c.2542T>G	NP_001350654.1:p.Ser848Ala
NM_001371656.1:c.4921T>G	NP_001358585.1:p.Ser1641Ala
NM_001374820.1:c.4921T>G	NP_001361749.1:p.Ser1641Ala
NM_001374828.1:c.5041T>G MANE Select	NP_001361757.1:p.Ser1681Ala
NM_017519.3:c.4882T>G	NP_059989.3:p.Ser1628Ala